SKU: 52911951990

ARR3 Recombinant Rabbit mAb (S-3290-27)

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Description

ARR3 Recombinant Rabbit mAb (S-3290-27)Product Specification Host Rabbit Antigen ARR3 Synonyms Arrestin C; Cone arrestin (C arrestin; cArr); Retinal cone arrestin 3; X arrestin; ARRX; CAR Immunogen Synthetic Peptide Location Cell projection Accession P36575 Clone Number S 3290 27 Antibody Type Recombinant mAb Isotype IgG Application IHC P Reactivity Hu Purification Protein A Concentration 0. 125 mg ml Conjugation Unconjugated Physical Appearance Liquid Storage Buffer PBS, 40% Glycerol, 0.

Product Specification


Host Rabbit
Antigen ARR3
Synonyms Arrestin-C; Cone arrestin (C-arrestin; cArr); Retinal cone arrestin-3; X-arrestin; ARRX; CAR
Immunogen Synthetic Peptide
Location Cell projection
Accession P36575
Clone Number S-3290-27
Antibody Type Recombinant mAb
Isotype IgG
Application IHC-P
Reactivity Hu
Purification Protein A
Concentration 0.125 mg/ml
Conjugation Unconjugated
Physical Appearance Liquid
Storage Buffer

PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, -20 °C as supplied

Dilution


application dilution species
IHC-P 1:2000 Hu

Background

ARR3 (Arrestin-C, also known as X-arrestin or Cone Arrestin) is a 45-kDa protein belonging to the arrestin family of regulatory proteins, specifically expressed in retinal cone photoreceptors and pinealocytes, where it plays a critical role in terminating G protein-coupled receptor (GPCR) signaling through high-affinity binding to light-activated, phosphorylated cone opsins. Structurally, ARR3 shares the characteristic two-domain arrestin fold with β-strand-dominated N- and C-domains connected by a flexible hinge region, enabling the protein to undergo a conformational change upon receptor engagement that precludes further G protein coupling while promoting receptor internalization and trafficking. Unlike the ubiquitously expressed ARR2 (β-arrestin-1) and ARR3's rod-specific counterpart SAG (S-antigen/arrestin-1), ARR3 demonstrates preferential affinity for short-wavelength cone opsins and exhibits distinct phosphorylation-dependent regulatory mechanisms that modulate its subcellular localization between the photoreceptor outer segment and synaptic terminal. Genetic mutations in the ARR3 gene have been associated with various retinal dystrophies, including Oguchi disease and certain forms of cone-rod dystrophy, underscoring its essential function in maintaining cone photoreceptor health and proper visual cycle regulation.

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SKU: 52911951990

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